HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-2-Chloroethane → 3,6-bis(2-chloroethoxy)-N-ethylcarbazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-2-Chloroethane | HCID 7849 | — |
| Reactant | Chlorobenzene | HCID 7964 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | N-ethyl-3,6-carbazolediol diacetate | HCID 12331788 | — |
| Product | 3,6-bis(2-chloroethoxy)-N-ethylcarbazole | HCID 21552329 | — |
Reaction Steps
To a stirred mixture of 31.3 g (0.1 mole) of N-ethyl-3,6-carbazolediol diacetate and 39.4 g (0.3 mole) of 1-bromo-2-chloroethane in 400 ml chlorobenzene is added 0.2 mole of sodium methoxide. Upon complete addition of the alkali, the mixture is refluxed with stirring for 18 hours, then cooled. The supernatant water layer is decanted and the residue is taken up in ethanol-chloroform to give 3,6-bis(2-chloroethoxy)-N-ethylcarbazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03947593 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-65da1e8c3e0940259ac6214293fb65f4 |
| Source note | uspto-grants-1976_03 |